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| 1 | DIGE compatible labelling of surface proteins on vital cells in vitro and invivo 显示文摘 | Mayrhofer C Krieger S Allmaier G | 2006 | Proteomics2006，6，2： | 1 |
| 2 | Characterisation of intact recombinant human erythropoietins applied in doping by means of planar gel electrophoretic techniques and matrix - assisted laser desorption/ionisation linear time - of - flight mass spectrometry显示文摘 | Gerald Sttibiger Martina Marchetti Marietta Nagano Christian Reichel ( tinter Gmeiner Gtinter Allmaier | 2005 | Rapid Communications in Mass Spectrometry2005，19，5： | 1 |
| 3 | DIGE compatible labelling of surface proteins on vital cells in vitro and in vivo显示文摘 | Mayrhofer C Krieger S Allmaier G Kerjaschki D | 2006 | Proteomics2006，6，2： | 1 |
| 4 | Mass spectrometry-one of the pillars of proteomics显示文摘 | Marchetti-Deschmann M Allmaier G | 2011 | J Proteomics2011，74，7： | 1 |
| 5 | Ecological Studies of Helicobaeter pylori 显示文摘 | Shahamate M cirillo D Allmaier G | 1989 | Klin Wochenschr1989，67，18： | 1 |
| 6 | Structural analysis ofBacillus subtilis 168 endospore peptidoglycan and its role duringdifferentiation显示文摘 | Atrih A ZSllneret P Allmaier G | 1996 | J Bacteriol1996，178，21： | 1 |
| 7 | Analysis and handling of bio-nanoparticles and environmental nanoparticles using electrostatic aerosol mobility显示文摘为在气压的 nanoparticles 的描述和操作的微分活动性分析的成功的应用程序产生了这种技术的进一步的开发。平行微分活动性分析器提供可能性同时测量 nanoparticles 的一个尺寸系列并且为收集与一种定义尺寸选择 nanoparticles 的一个特别集合(象丰富一样) 并且进一步直角的分析(至于例子电子显微镜学,原子力量显微镜学或集体 spectrometry ) 。执行电的活动性直径的高分辨率大小允许种类的分子的重量决心与超离频在大多尔顿的分子的群众变化(例如蛋白质建筑群) 。人的鼻病毒的精确尺寸测量证实了这种技术的潜力分析甚至未经触动的传染人病原的病毒。而且,在城市的环境的 nanoparticle 出现的即时测量在重要性的另外的区域也证实这里介绍的方法和它的适用性的通用性。 | Peter Kallinger Victor U.Weiss Angela Lehner Gunter Allmaier Wladyslaw W.Szymanski | 2013 | Particuology2013，11，1： | 1 |
| 8 | Re- fined simulation of friction power loss in crank shaft slider bearings considering wear in the mixed lubrication regime 显示文摘 | PRIESTNER C ALLMAIER H PRIEBSCH H | 2012 | Tribology International2012，46，： | 1 |
| 9 | Insight into degradation of ammonium-based ionic liquids and comparison of tribological performance between selected intact and altered ionic liquid显示文摘 | Lucia Pisarova Vladimir Totolin Christoph Gabler Nicole D?rr Ernst Pittenauer Günter Allmaier Ichiro Minami | 2013 | Tribology International2013，，： | 1 |
| 10 | DIGE compatible labeling of surface proteins on vital cells in vitro and in vivo显示文摘 | MAYRHOFER C KRIEGER S ALLMAIER G | 2006 | Proteomies2006，6，2： | 1 |
| 11 | Re- fined Simulation of friction power loss in crank shaft slider bearings considering wear in the mixed lubrica- tion regime显示文摘 | Priestner C Allmaier H Priebsch H H | 2012 | Tribology International2012，46，1： | 1 |
| 12 | Predicting friction reliably and accurately in journal bearings-Ex- tending the EHD simulation model to TEHD显示文摘 | Allmaier H Priestner C Reich F M | 2013 | Tri- bology International2013，58，： | 1 |
| 13 | MALDI-TOF mass spectrometry imaging reveals molecular level changes in ultrahigh molecular weight polyethylene joint implants in correlation with lipid adsorption显示文摘 | SOPHIE M MARIA V ALLMAIER G | 2014 | Analytical Chemistry2014，86，19： | 1 |
| 14 | Transposition of group Ⅱ intron aI1 in yeast and invasion of mitochondrial genes at new locations显示文摘 | Mueller M W Allmaier M Eskes R | 1993 | Nature1993，366，6451： | 1 |
| 15 | Molecular weight determination of ultra-high mass compounds on a standard matrix-assisted laser desorption/ioniza- tion time-of-flight mass spectrometer: PAMAM dendrimer generation 10 and immunoglobulin M 显示文摘 | MULER R ALLMAIER G | 2006 | Rapid Communications in Mass Spectrome- try2006，20，24： | 1 |
| 16 | Development of a sample preparation approach to measure the size of nanoparticle aggregates by electron microscopy显示文摘Electron microscopy (EM) is widely used for nanoparticle (NP) sizing. Following an initial assessment of two sample preparation protocols described in the current literature as'unperturbed', we found that neither could accurately measure the size of NPs featuring a broad size distribution, e.g., aggregates. Because many real-world NP samples consist of aggregates, this finding was of considerable concern. The data showed that the protocols introduced errors into the measurement by either inducing agglomeration artefacts or providing a skewed size distribution towards small particles (skewing artefact). The focus of this work was to develop and apply a mathematical refinement to correct the skewing artefact. This refinement provided a much improved agreement between EM and a reference methodology, when applied to the measurement of synthetic amorphous silica NPs. Further investigation, highlighted the influence of NP chemistry on the refinement. This study emphasised the urgent need for greater and more detailed consideration regarding the sample preparation of NP aggregates to routinely achieve accurate measurements by EM. This study also provided a novel refinement solution applicable to the size characterisation of silica and c让rate-coated gold NPs featuring broad size distributions. With further research, this approach could be extended to other NP types. | Agnieszka Dudkiewicz Angela Lehner Qasim Chaudhry Kristian Molhave Guenter Allmaier Karen Tiede Alistair B.A. Boxall Peter Hofmann John Lewis | 2019 | Particuology2019，17，4： | 0 |
| 17 | Nanoscale chemical imaging of individual chemotherapeutic cytarabineloaded liposomal nanocarriers显示文摘Dosage of chemotherapeutic drugs is a tradeoff between efficacy and side-effects.Liposomes are nanocarriers that increase therapy efficacy and minimize side-effects by delivering otherwise difficult to administer therapeutics with improved efficiency and selectivity.Still,variabilities in liposome preparation require assessing drug encapsulation efficiency at the single liposome level,an information that,for non-fluorescent therapeutic cargos,is inaccessible due to the minute drug load per liposome.Photothermal induced resonance (PTIR) provides nanoscale compositional specificity,up to now,by leveraging an atomic force microscope (AFM) tip contacting the sample to transduce the sample's photothermal expansion.However,on soft samples (e.g.,liposomes) PTIR effectiveness is reduced due to the likelihood of tip-induced sample damage and inefficient AFM transduction.Here,individual liposomes loaded with the chemotherapeutic drug cytarabine are deposited intact from suspension via nano-electrospray gas-phase electrophoretic mobility molecular analysis (nES-GEMMA) collection and characterized at the nanoscale with the chemically-sensitive PTIR method.A new tapping-mode PTIR imaging paradigm based on heterodyne detection is shown to be better adapted to measure soft samples,yielding cytarabine distribution in individual liposomes and enabling classification of empty and drug-loaded liposomes.The measurements highlight PTIR capability to detect ~ 103 cytarabine molecules (~ 1.7 zmol) label-free and non-destructively. | Karin Wieland Georg Ramer Victor U. Weiss Guenter Allmaier Bemhard Lendl Andrea Centrone | 2019 | Nano Research2019，12，1： | 0 |
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